Literature DB >> 28221266

Body Mass Index and the Association With Vaso-occlusive Crises in Pediatric Sickle Cell Disease.

Andrea Zivot1, Nataly Apollonsky, Edward Gracely, Deepti Raybagkar.   

Abstract

BACKGROUND: Children with sickle cell disease (SCD) historically have been underweight and have poor overall growth. Recent studies have demonstrated a trend toward obesity in pediatric SCD populations.
MATERIALS AND METHODS: Through retrospective chart review of patients with SCD followed at our center, we collected patient's data, including body mass index (BMI), weight percentiles, sickle cell genotype, baseline hemoglobin, medical and psychiatric comorbidities, 25-hydroxy vitamin D level, treatment with hydroxyurea, and chronic transfusions. We identified hospitalizations to St. Christopher's Hospital for vaso-occlusive crisis (VOC) and duration of hospitalization and intravenous opioid use were recorded. Student t test, Mann-Whitney U test, and analysis of variance were used to examine associations between variables and frequency and duration of hospitalizations for VOC.
RESULTS: Among 328 patients with SCD, overweight and obese children constituted 19% of hospitalized and nonhospitalized patients. BMI status did not influence frequency (P=0.90) or duration of hospitalization (P=0.65) for VOC. Obesity was more associated with HbSC than HbSS (P=0.025) genotype.
CONCLUSIONS: Our study did not demonstrate an association between extremes of BMI of patients and hospitalization for VOC. Considering current trend toward obesity, further prospective and interventional research are required to define the effects of extremes of BMI on pain crises in SCD.

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Year:  2017        PMID: 28221266     DOI: 10.1097/MPH.0000000000000787

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  4 in total

1.  Impact of Bariatric Surgery on Outcomes of Patients with Sickle Cell Disease: a Nationwide Inpatient Sample Analysis, 2004-2014.

Authors:  Prabin Sharma; Thomas R McCarty; Siddhartha Yadav; Julius N Ngu; Basile Njei
Journal:  Obes Surg       Date:  2019-06       Impact factor: 4.129

2.  Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.

Authors:  Ambroise Wonkam; Khuthala Mnika; Valentina J Ngo Bitoungui; Bernard Chetcha Chemegni; Emile R Chimusa; Collet Dandara; Andre P Kengne
Journal:  Br J Haematol       Date:  2017-12-03       Impact factor: 6.998

3.  Weight status and health behaviors of adolescents and young adults with sickle cell disease: The emerging risk for obesity.

Authors:  Heather Strong; Onengiya Harry; Emilie Westcott; Katherine M Kidwell; Sarah C Couch; Abigail Peairs; Maria T Britto; Lori E Crosby
Journal:  Pediatr Hematol Oncol       Date:  2020-11-05       Impact factor: 2.070

4.  High body mass index in children with sickle cell disease: a retrospective single-centre audit.

Authors:  Rachael Hall; Kate Gardner; David C Rees; Subarna Chakravorty
Journal:  BMJ Paediatr Open       Date:  2018-10-23
  4 in total

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